Canonical Allele Identifier: CA2723946422

Gene: TCN1

Linked Data

• dbSNP Id: rs2134515809

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.59865920C>G , CM000673.2:g.59865920C>G	GRCh38
NC_000011.9:g.59633393C>G , CM000673.1:g.59633393C>G	GRCh37
NC_000011.8:g.59389969C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000257264.4:c.79+472G>C MANE Select	ENSP00000257264.3:n.79+472G>C
ENST00000257264.3:c.79+472G>C	ENSP00000257264.3:n.79+472G>C
ENST00000532419.5:n.98+472G>C
ENST00000534531.1:n.80+472G>C
NM_001062.3:c.79+472G>C	NP_001053.2:n.79+472G>C
NM_001062.4:c.79+472G>C MANE Select	NP_001053.2:n.79+472G>C